Acetic acid, [(4-nitrophenyl)sulfonyl]-, phenylmethyl ester

Base Information

Chemical Name:Acetic acid, [(4-nitrophenyl)sulfonyl]-, phenylmethyl ester
CAS No.:151194-84-2
Molecular Formula:C15H13NO6S
Molecular Weight:335.337
Hs Code.:
DSSTox Substance ID:DTXSID80476325
Nikkaji Number:J1.635.380I
Wikidata:Q82307468

Synonyms:Acetic acid, [(4-nitrophenyl)sulfonyl]-, phenylmethyl ester;151194-84-2;DTXSID80476325

Suppliers and Price of Acetic acid, [(4-nitrophenyl)sulfonyl]-, phenylmethyl ester

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of Acetic acid, [(4-nitrophenyl)sulfonyl]-, phenylmethyl ester

Chemical Property:

XLogP3:2.4
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:6
Exact Mass:335.04635831
Heavy Atom Count:23
Complexity:507

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)COC(=O)CS(=O)(=O)C2=CC=C(C=C2)[N+](=O)[O-]

Technology Process of Acetic acid, [(4-nitrophenyl)sulfonyl]-, phenylmethyl ester

There total 5 articles about Acetic acid, [(4-nitrophenyl)sulfonyl]-, phenylmethyl ester which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 47.0%

: 533888-69-6
benzyl [(4-nitrophenyl)thio]acetate

: 151194-84-2
benzyl [(4-nitrophenyl)sulfonyl]acetate

Guidance literature:: With Oxone; In methanol; water; at 20 ℃; for 24h;
DOI:10.1002/hlca.200290013

Reference yield:

: 1849-36-1
para-nitrobenzenethiol

: 151194-84-2
benzyl [(4-nitrophenyl)sulfonyl]acetate

Guidance literature:: Multi-step reaction with 2 steps

1: NaH / acetonitrile / 20 °C

2: Oxone(R) / CH₂Cl₂ / 24 h / 20 °C

With oxone; sodium hydride; In dichloromethane; acetonitrile;
DOI:10.1016/S0040-4039(01)01920-7

Reference yield:

: 5437-45-6
Benzyl bromoacetate

: 151194-84-2
benzyl [(4-nitrophenyl)sulfonyl]acetate

Guidance literature:: Multi-step reaction with 2 steps

1: NaH / acetonitrile / 20 °C

2: Oxone(R) / CH₂Cl₂ / 24 h / 20 °C

With oxone; sodium hydride; In dichloromethane; acetonitrile;
DOI:10.1016/S0040-4039(01)01920-7